GMP Project Manager
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Gentofte
Are you passionate about quality and compliance and continuously improving the quality culture and would you like to become a part of a global community that values diversity, innovation, and growth?
If yes, this is a great opportunity to build and improve the business and to be part of defining the department and connecting with people.
Apply now and join us as our new GMP project manager.
The position
As a GMP Project Manager, you will work across the Biotech & Rare Disease (BRD) Active Pharmaceutical Ingredient (API) area in DK and you will report to the director of BRD API DK Business Support.
In close collaboration with the management group, you will be responsible for always securing product quality and inspection readiness. Furthermore, with local GMP coordinators and cLEAN partners you will be responsible for continuously improving the quality culture and systems in BRD API DK productions.
Your main tasks will be focused on:
• Driving the implementation, integration and coordination of projects coming from NN Global Quality, e.g., as CVP implementation lead for “data integrity”
• Developing strategies, implement, and follow up on quality problems
• Developing cross functional systems and standards for quality and compliance
• Leading and drive the GMP coordinator group in BRD API DK and help develop a network across LEAN, GMP and training
• Securing regular and pro-active input and inspiration to the management team
You will be covering our GMP Partner who is on a maternity leave and after that you will start covering other projects related to BRD.
Joining our department means stepping into a role where you will play a vital part in defining further development of BRD API DK and BRD API DK Business Support.
Qualifications
To be a competitive candidate, you should have:
• A MSc degree related to Life Science, Engineering, Business, or any other related field and several years of experience with GMP, compliance, quality
• Project management and change management experience
• Six Sigma experience would be an advantage
• Science and Risk based Validation (SRV) experience
• Experience in a manufacturing environment, preferably within GMP and manufacturing processes
• Professional proficiency in English. Danish would be an advantage
On a personal level, you have an analytical and curious mindset, a high ability to navigate in complex stakeholder landscape and matrix organization and you negotiate at all levels in the organization.
You are motivated by challenging assignments, and you absorb new knowledge quickly, demonstrating great cooperation skills, and your proficiency lies in fostering collaboration and ensuring engagement among other employees while setting the overall Strategic direction.
About the department
BRD API (Active Pharmaceutical Ingredient) Denmark is part of BRD. At our sites in Gentofte, Hillerød, and Kalundborg, we are more than 600 colleagues working together to manufacture the API used in life-saving medicine for people living with serious chronic diseases. We work with advanced chemical and biotechnological processes such as cultivation, recovery, purification, and freeze-drying. We bring value to our patients by providing the cleanest possible high-quality API made in accordance with Good Manufacturing Practice (GMP) while constantly optimising our processes.
Working at BRD, Novo Nordisk
BRD is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. In BRD, we are not only supplying all Novo Nordisk products to people living with serious chronic diseases, but we also use our competences in biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk.
We are more than 3000 dedicated colleagues working at six production sites in Denmark and the United States. Here we cover the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. As more and more people need our products, we support Novo Nordisk's initiatives in new therapy areas. Every day, we work to streamline and expand our capacity through process innovation, automation, and the introduction of new technology.
Contact
For further information, please contact Business Support Director, Lene Madsen (LMAD) at +45-30758342
Deadline
28 January 2024
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
If yes, this is a great opportunity to build and improve the business and to be part of defining the department and connecting with people.
Apply now and join us as our new GMP project manager.
The position
As a GMP Project Manager, you will work across the Biotech & Rare Disease (BRD) Active Pharmaceutical Ingredient (API) area in DK and you will report to the director of BRD API DK Business Support.
In close collaboration with the management group, you will be responsible for always securing product quality and inspection readiness. Furthermore, with local GMP coordinators and cLEAN partners you will be responsible for continuously improving the quality culture and systems in BRD API DK productions.
Your main tasks will be focused on:
• Driving the implementation, integration and coordination of projects coming from NN Global Quality, e.g., as CVP implementation lead for “data integrity”
• Developing strategies, implement, and follow up on quality problems
• Developing cross functional systems and standards for quality and compliance
• Leading and drive the GMP coordinator group in BRD API DK and help develop a network across LEAN, GMP and training
• Securing regular and pro-active input and inspiration to the management team
You will be covering our GMP Partner who is on a maternity leave and after that you will start covering other projects related to BRD.
Joining our department means stepping into a role where you will play a vital part in defining further development of BRD API DK and BRD API DK Business Support.
Qualifications
To be a competitive candidate, you should have:
• A MSc degree related to Life Science, Engineering, Business, or any other related field and several years of experience with GMP, compliance, quality
• Project management and change management experience
• Six Sigma experience would be an advantage
• Science and Risk based Validation (SRV) experience
• Experience in a manufacturing environment, preferably within GMP and manufacturing processes
• Professional proficiency in English. Danish would be an advantage
On a personal level, you have an analytical and curious mindset, a high ability to navigate in complex stakeholder landscape and matrix organization and you negotiate at all levels in the organization.
You are motivated by challenging assignments, and you absorb new knowledge quickly, demonstrating great cooperation skills, and your proficiency lies in fostering collaboration and ensuring engagement among other employees while setting the overall Strategic direction.
About the department
BRD API (Active Pharmaceutical Ingredient) Denmark is part of BRD. At our sites in Gentofte, Hillerød, and Kalundborg, we are more than 600 colleagues working together to manufacture the API used in life-saving medicine for people living with serious chronic diseases. We work with advanced chemical and biotechnological processes such as cultivation, recovery, purification, and freeze-drying. We bring value to our patients by providing the cleanest possible high-quality API made in accordance with Good Manufacturing Practice (GMP) while constantly optimising our processes.
Working at BRD, Novo Nordisk
BRD is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. In BRD, we are not only supplying all Novo Nordisk products to people living with serious chronic diseases, but we also use our competences in biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk.
We are more than 3000 dedicated colleagues working at six production sites in Denmark and the United States. Here we cover the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. As more and more people need our products, we support Novo Nordisk's initiatives in new therapy areas. Every day, we work to streamline and expand our capacity through process innovation, automation, and the introduction of new technology.
Contact
For further information, please contact Business Support Director, Lene Madsen (LMAD) at +45-30758342
Deadline
28 January 2024
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Gentofte.
Jobbet er oprettet på vores service den 12.1.2024, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Øvrige
- Gentofte
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Statistik over udbudte jobs som øvrige i Gentofte
Herunder ser du udviklingen i udbudte øvrige i Gentofte over tid. Bemærk at jobs der ikke har en bestemt geografi ikke er medtaget i tabellen. I den første kolonne ser du datoen. I den næste kolonne ser du det samlede antal øvrige.
Se flere statistikker her:
Statistik over udbudte øvrige i Gentofte over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 22. november 2024 | 24 |
| 21. november 2024 | 23 |
| 20. november 2024 | 22 |
| 19. november 2024 | 21 |
| 18. november 2024 | 17 |
| 17. november 2024 | 17 |
| 16. november 2024 | 19 |
| 15. november 2024 | 21 |
| 14. november 2024 | 19 |
| 13. november 2024 | 20 |
| 12. november 2024 | 21 |
| 11. november 2024 | 22 |
| 10. november 2024 | 22 |
| 9. november 2024 | 22 |
| 8. november 2024 | 20 |
| 7. november 2024 | 18 |
| 6. november 2024 | 17 |
| 5. november 2024 | 15 |
| 4. november 2024 | 19 |
| 3. november 2024 | 19 |
| 2. november 2024 | 19 |
| 1. november 2024 | 19 |
| 31. oktober 2024 | 17 |
| 30. oktober 2024 | 16 |
| 29. oktober 2024 | 16 |
| 28. oktober 2024 | 16 |
| 27. oktober 2024 | 18 |
| 26. oktober 2024 | 18 |
| 25. oktober 2024 | 16 |
| 24. oktober 2024 | 19 |
| 23. oktober 2024 | 20 |